食品科学 ›› 2026, Vol. 47 ›› Issue (6): 49-57.doi: 10.7506/spkx1002-6630-20251014-074

• 基础研究 • 上一篇    

氧化白藜芦醇和抗坏血酸协同抑制多酚氧化酶机制

刘若冰,杜纤纤,任志强,刘佩,张耸,彭勇   

  1. (山东农业大学食品科学与工程学院,山东 泰安 271018)
  • 发布日期:2026-04-14
  • 基金资助:
    山东省重点研发计划项目(2024TZXD044;2024TZXD043);国家自然科学基金青年科学基金项目(32302178)

Mechanism of Synergistic Inhibition of Oxyresveratrol and Ascorbic Acid on Polyphenol Oxidase

LIU Ruobing, DU Qianqian, REN Zhiqiang, LIU Pei, ZHANG Song, PENG Yong   

  1. (College of Food Science and Engineering, Shandong Agricultural University, Tai’an 271018, China)
  • Published:2026-04-14

摘要: 为探究氧化白藜芦醇(oxyresveratrol,OXY)与抗坏血酸(ascorbic acid,AA)协同抑制多酚氧化酶(polyphenol oxidase,PPO)的机制,本研究通过抑制率测定、动力学分析、分子对接及结构表征等方法系统评价其协同效应。结果表明,OXY和AA协同处理能够显著抑制鲜切马铃薯丝的褐变和PPO活性,其中OXY与AA以2∶1体积比复配时协同效果最佳,其PPO抑制率比单一OXY和AA处理分别提高9.08%和38.12%,铜离子螯合能力比单一OXY和AA处理提高41.07%和135.45%。动力学分析表明,协同处理属于混合型抑制,对游离PPO和对酶-底物复合物的抑制常数分别为2.46 μmol/L和3.27 μmol/L。分子对接结果表明,协同处理的OXY-AA-PPO复合物所形成氢键数量增加,且与单一处理相比,协同处理的结合能分别降低2.32、4.45 kcal/mol,其蛋白构象稳定性增强。荧光光谱和圆二色光谱分析也表明,OXY和AA以2∶1体积比复配时发射荧光强度为原酶的71.93%,其β-折叠结构的相对含量分别比单一处理分别减少了20.2%、10.4%,证实协同作用通过破坏酶的三级结构和二级结构实现。本研究可为协同抑制技术在鲜切果蔬保鲜方面的应用提供参考。

关键词: 氧化白藜芦醇;抗坏血酸;多酚氧化酶;协同抑制;荧光光谱

Abstract: To investigate the mechanism of synergistic inhibition of oxyresveratrol (OXY) and ascorbic acid (AA) on polyphenol oxidase (PPO), this study systematically evaluated their synergistic effects through the determination of inhibition rates, kinetic analysis, molecular docking, and structural characterization. The results showed that the synergistic treatment of OXY and AA significantly inhibited the browning of fresh-cut potato strips and reduced the activity of PPO, with the most pronounced effect observed at a OXY:AA volume ratio of 2:1. The inhibition rate of PPO increased by 9.08% and 38.12% compared with individual treatments with OXY or AA, respectively. Additionally, the chelation capacity of copper ion was enhanced by 41.07% and 135.45% compared with the individual treatments, respectively. Kinetic analysis revealed that the synergistic inhibition followed a mixed-type mechanism, with inhibition constants for free PPO and enzyme-substrate complexes of 2.46 and 3.27 μmol/L, respectively. Molecular docking results indicated that the OXY-AA-PPO complex formed more hydrogen bonds under synergistic conditions, and the binding energy decreased by 2.32 and 4.45 kcal/mol compared with the individual treatments, respectively, suggesting improved protein conformational stability. Fluorescence spectroscopy and circular dichroism (CD) spectroscopy further demonstrated that the emission fluorescence intensity of PPO treated with the 2:1 combination was 71.93% of that of the original enzyme, and the β-sheet content decreased by 20.2% and 10.4%, respectively, compared with the individual treatments, confirming that the synergistic effect disrupted the tertiary and secondary structures of the enzyme. This study provides a reference for the application of synergistic inhibition technology in the preservation of fresh-cut fruits and vegetables.

Key words: oxyresveratrol; ascorbic acid; polyphenol oxidase; synergistic inhibition; fluorescence spectroscopy

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